chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7125048666125048667TC13GENIChomozygous54095975
7125048786125048787GA16GENICheterozygous54751193
7125048936125048937GT12GENICpossibly homozygous54095976
7125049753125049759CAAAAA------3GENICheterozygous54751195
7125050478125050479GT17GENIChomozygous54095985
7125052214125052215TTGGAG2GENIChomozygous54095989
7125054097125054098GC12GENIChomozygous54751201
7125055836125055837GC2GENICheterozygous54751203
7125055845125055846AG2GENIChomozygous54095994
7125055846125055847TTG1GENIChomozygous54751205
7125055851125055852AG2GENIChomozygous54095995
7125057462125057463AG4GENIChomozygous54095997
7125057782125057783CT8GENIChomozygous54751207
7125058254125058255CT9GENICpossibly homozygous54751209
7125058519125058520TC10GENIChomozygous54095998
7125059731125059732GGC5GENIChomozygous54096000
7125062164125062165GA8GENIChomozygous54751211
7125063395125063396GA10GENICpossibly homozygous54751213
7125063555125063556T-4GENICheterozygous54096015
7125063609125063610GA7GENIChomozygous54751215
7125065231125065232TC8GENICpossibly homozygous54096018
7125066925125066926GC2GENIChomozygous54096020
7125066951125066952TA4GENIChomozygous54751217
7125068721125068722TC13GENICpossibly homozygous54096027
7125070527125070528TG9GENIChomozygous54096029